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I’d like to say I’m a consummate reader as though I read Dickens and Faust and thought-provoking interviews and opinion pieces about the state of our world and current affairs. And sometimes, I do. But when I say I’m a consummate reader I mean I read a lot … of everything.
Which includes, but is not limited to, daily email blasts and articles from Mind Body Green.
It was one of these articles that started niggling in my head until I felt I had no choice but to give it the attention it felt it was due.
Which is how I have found myself pledging to cook all our meals for the entire month of October.
Wait, wha?
I have read many articles on various diets, both fad and health-related. I have read about Paleo and Keto and the benefits and drawbacks of vegetarian and vegan lifestyles. I have read about the Wahl’s Protocol and OMS (Overcoming Multiple Sclerosis). I have read articles (upon articles) about the benefits of various food groups or individual foods helping with specific issues (um, inflammation, I’m looking at you).
But …. I’m also a little bit of a cynic. In addition to being wildly stubborn and pouty.
What I loved about the article I read was the idea that sometimes, we lose track of our food and how we are consuming it. Life gets busy, it gets stressful, there aren’t enough hours in the day. And take-out or ready-made food is a really great solution. Which maybe we think we only do once in awhile, but then all of a sudden, I’m getting sushi take-out twice a week. Not only do I need a second mortgage to afford all the sushi, but something is getting lost nutritionally.
The author also wrote about how relaxing it was to get home and prepare meals with her husband. I think that’s what really hooked me. Because when the hubs and I do make dinner and stand together chopping vegetables or prepping fish or meat for the grill, we talk and laugh and interact in a way that is far healthier than sitting beside each other scrolling through our phones as our pre-made dinner cooks in the oven.
And then there was the idea that just cooking fresh food could actually be healthier than any kind of restriction or diet. That the act of cooking meant that I would know exactly what went into it, I could control the portion sizes and I would be responsible for what went into my body. Every day. It wouldn’t be about counting cups of dark leafy vegetables or measuring fat grams. It would be about eating whole, healthy food prepared daily by yours truly.
I was really into this idea. And so, to keep myself accountable, I thought why not revisit the roots of this blog, and share my cooking adventures through the month of October?
If you’d like to read the article that inspired me, you can find it below (along with the rules she outlines!). So … here goes!
https://www.mindbodygreen.com/articles/budget-30-day-home-cooking-challenge
injury time out
On Sunday I was walking down the stairs to take Lucy out and my right foot slipped. It slid four or five steps. My left did not. There were bumps and John came running. I looked up at him with teary eyes and smiled, nodding slightly. “I just slipped,” I said, but the tears weren’t because of that.
He told me not to move, he would take Lucy out. Normally, I would agree and then blatantly ignore him. But I didn’t. After getting both legs next to each other (from their lightening bolt position of the slip) I sat and waited for him to come home. I tried to feel as much as I could in my legs. Which, if I’m honest, isn’t much. Even on a good day.
A million thoughts raced through my head. Breath steady and move your toes and just be quiet for a minute. Those were the good thoughts. The bad ones included It’s your knee, how you could have been so stupid, it will take ten times the amount of time to heal because of MS ….
But I walked upstairs when John got home. We iced it. We went to bed. I felt confident that it would be okay.
On Monday we went to the ER. Because it didn’t feel okay. It felt wretched and scary and I felt wretched and scared (and frustrated and mad and defeated … among other things). The ER told us (after hours and ex-rays and the sound of sneakers on linoleum passing our room over and over) a whole lot of nothing. As we drove home in the rain of Hurricane Florence I spewed vitriol, frustrations dripping in sarcasm and resentment.
Life isn’t always about having MS. But also … it is always about having MS.
This week has been brutal for me. Drowning in my frustrations, my limitations, the pain of my body from inactivity as much as injury. Resentment. Inability. The list goes on, and on. And infuriatingly on.
The truth? I will take longer to heal than someone who doesn’t have an autoimmune disease. I will also be slightly more proactive about it, because I know how debilitating the consequences are for not taking care of myself.
I didn’t fall down the stairs because of MS. So as mad as I’ve been, I can’t blame it on my disease. I slipped on the steps because I didn’t have shoes on, I was looking behind me to get Lucy to come down the stairs and I missteped. Not being able to blame MS pisses me off, to be honest. I like when MS gets to be the bad guy of my life. I wasn’t super pleased at having to accept that this slip could have happened to anyone, MS or not.
It is challenging to be restricted. It’s challenging to have to sit, knowing full well that the only thing that will help things get better is time. It’s challenging to go to sleep each night trying to figure out how to get the best rest possible when it feels impossible. Not being able to run around and do simple household chores means that all I can do is sit here and think about it. Think about life. Think (and worry) about my knee. Think about everything I currently can’t do.
It’s also hard to acknowledge all the challenges, admit your faults and move through it. I am pretty bad at that. Today, as the week winds down into the weekend, the only thing I am trying to do is give myself a break. Let go of the resentment. Accept everything for what it is without needing to define or categorize it. And breathe through it.
That’s really all I can do.
change
My life has changed dramatically since leaving my job last January.
I mean, dramatically.
At first, I felt lost. As though I had no direction and even worse, didn’t even know how to find one. Then I felt resentful. At the circumstances under which I left my job. At my disease. At the world for doing me so dirty. And then came defiance. I will conquer. I will succeed. I will create and live and be unstoppable.
But MS nipped that one pretty quickly in the bud.
Who am I? What do I want to do with my life? What am I currently doing with my life? … I chewed on these questions for a long time. I felt like I wasn’t contributing to our household, that I was the weak link. That this invisible illness of mine was debilitating, but not debilitating *enough*.
But the real question that I kept coming back to was ~ who was I before and why was I that girl? Did I like that girl? Was I proud of her? Did she pursue dreams relentlessly and with passion? Um…. hmmm.
I spent a lot of time not knowing myself and not really having a clear direction (other than stay alive and pay the bills). I spent over twenty years in the hospitality/restaurant industry because I sort of landed there. And I did love it. And I was passionate about it. I was so proud of my last company and all it accomplished while I was there. I look at it now and it’s nearly unrecognizable — it just blew up. Which is fabulous. But I’m not sad that I’m no longer part of it. I wasn’t *that* passionate.
I went to college for musical theatre. And I absolutely adore musical theatre. In fact, I was medium okay at performing, too. But I wasn’t passionate enough to risk it all. To sleep on couches and starve myself and do everything you need to do to make it in the industry. I started waiting tables instead. (See above for where that lead).
So you can imagine that these past eighteen months have been interesting for me. Challenging, frustrating, desperate. Freeing.
I mean, seriously. What do I care about?
Last year was a blur. I quit and then John had surgery. Then he started a new job. And then September happened and September to December are always a blur of football and holidays. This year started well – we hosted our first Rabbie Burns supper and I was hired by Aflac to sell insurance. I got my license. I did my training. I f*cking hated it. I had some major issues with how business was done. I lasted a month. It wasn’t my finest moment in time.
And then the husband told me to go back to yoga.
He’d said it in the past but he was pretty adamant this time. My body was hurting. I was riding my bike every day but I was getting stiffer. The relief that I’d experienced before this for all the joyous physical MS symptoms was fading. I was mentally trapped. And then Dr. Markowitz suggested in April that I needed to figure out my anxiety because my MS wasn’t being triggered by anything physical. Physically, he said, I was doing really well.
Well, isn’t that a b*tch.
Timing is a crazy thing. I received an email blast from a new yoga studio offering a new student special – $21 for 21 days. I called my friend (recently on short term disability for a new MS drug therapy) and we began our 21 days. She didn’t end up staying at the studio after those first few weeks. But I did. I had found something that was missing. I still don’t know if I can put my finger on what it is. But I found it. And it led to some amazing things.
First, it led me to the chiropractor. I did something to my left shoulder (always a painful nuisance … thank you high school swim team). I arrived at my chiro slightly trepidatious but over my first three months fell madly in love with their philosophies, their clean living examples (homemade bug spray! homemade sunscreen! detox diets!)and their long term goal of helping me be the healthiest version of myself I can be.
I discovered essential oils. With a healthy dose of skepticism I ordered a diffuser and all kinds of oils I didn’t even understand. I didn’t even know how to use them for the first few weeks. I just occasionally googled something and then went about my day. And then, all of sudden, things started to make sense.
I also fully committed to using more natural products. I mean, your skin is your largest organ. It makes sense that the things you put on it affect your body as a whole. But I’m a skincare snob. I mean, a big one. Finding new products was not something I undertook lightly.
But Instagram came to my rescue (as it so often does … sort of, haha!). I found Real Simple Soaps out of Hilton Head Island South Carolina and I fell so ridiculously in love with her products that I even got my mother on the natural products train. RSS makes products using goat milk, kefir and probiotics with all natural ingredients. And the stuff works better than anything I’ve ever used. This amazing discovery led me to try Kopari deodorant (all natural coconut). Once the door to vegan, non-GMO, cruelty-free, natural products was open, I not only discovered some amazing things (all Kopari products that I’ve tried are amazing and Thrive Causmetics are THE SH*T) but I felt really, really happy.
I also took Dr. M’s advice and went to therapy. That has been super interesting. Always rewarding, sometimes painful. Usually thought-provoking.
I think that what I’ve learned more clearly than anything I expected to learn was the empowering and positive force of self care. It sounds super (I mean, super duper) pretentious, but it isn’t. I believe in it passionately. I believe in getting sweaty every day and the cleansing power of physically moving your body. I believe in eating healthy, whole foods (but still uber delicious and fun and inventive and non-restrictive). I believe in drinking a ton of water. I mean, a ton. (I drink about 96 ounces a day. I know. It’s a lot). I believe in prioritizing sleep in order to more fully enjoy your awake hours.
I have found that taking care of myself is so much more than getting my Tysabri infusion every twenty-eight days. And in turn, it helps keep my MS under control. It’s insanely powerful.
So I might not have a clear direction yet. But I’m starting to get a good sense of what I believe in, what I’m passionate about and how I want to spend my time. I’m learning to love and accept myself, flaws and all. I’m learning to forgive myself and my disease for bad days.
I’m also attempting to learn how to have curly hair. It’ll be an adventure.
some poetry (oh, fancy!)
A few things I’ve written over the years. Poetry is certainly not my strong suite. But every once in awhile, something rhythmic happens in my brain.
i. 6.29.16
I am drowning in a sea of self-destruction
Walking through memories best forgotten
Who I was, who I am … how I came to be
So much pain, so much angst, so much misery
And on the other side, in the sun, in the light
How much should I remember, and how much release to flight?
I am angry, I am resigned. I am strong, I am kind.
I was not always who I am today.
And *that* for now, must be okay.
ii. 2.17.17
I am breathing
Like a rhythm
My heart, my lungs, my soul
I am searching for an answer
to a question
I don’t know …
I am reaching
for your hand
For something I can hold
I am praying
for an answer
to the swirling of my world
iii. 11.16.99
I’m battered, I’m bruised
I’m aching, I’m used
I’m broken, I’m breathless
I’ve fallen, you’re gone
I’m shut down, inside out
Silent, consumed with doubt
Waiting in darkness, in misery
And it would take a stronger person than I could ever be
To take on the challenge of me
To lift me higher than I’ve ever been
To make me believe again
deja vu
I remember the first time I went to NIH for a surgery. John & I took his father down, spent the day in the surgical waiting room and were able to see Alan in the ICU that evening as he crawled out of anesthesia and began working on recovery.
I’ve done it twice now with John, deliriously tired, pacing a hospital I have come to know. Watching the clock. Reminding myself not to panic. Finally finding my husband in ICU, his face flushed and his words groggy. But back.
This past Friday John and I celebrated our fifth wedding anniversary. Our tenth year of togetherness. Time is a strange and wonderful phenomenon. “This too shall pass’ is one of the truest sayings that exists. ‘Time heals all’. Another good one.
But sometimes things circle around and you find yourself facing the same demons you’ve conquered in the past. This morning we woke up at 3am (I use ‘woke up’ loosely because I’m still not sure I’m awake) and journeyed to Elmira, NY for Alan’s latest surgery. And we are in another surgical waiting room. Eating fast food. Waiting. Bleary-eyed.
The waiting is the worst.
Nothing makes the time go faster. And as it slips past (slower than usual) it feels painfully wasted and, conversely, painfully important.
In the end, we are all small beings moving through our small lives with their ups and downs and twists and turns. Nothing occurring will be remembered in 100 years or prove to be significant in any way. Which makes the significance in this moment, to these people (myself included) heartbreakingly poignant.
Did I mention I was tired? Yes. Very tired.
Also introspective, contemplative.
We each shape our stories with our attitudes, our thoughts, our beliefs. The things we place value in, the way we choose to articulate ourselves. We can be positive, negative, optimistic, realistic, pessimistic. We can find comfort or insult in any action. We have been gifted the divine right to choose.
Today feels like deja vu. And also, nothing like deja vu. As my shoulders and back burn & ache from fatigue. And my eyelids lay heavily across my pupils. And I’m intermittently bone-numbingly cold and uncomfortably stale & warm.
I need to sleep. And sweat. And stretch. And drink green smoothies or juice — or anything that feels nutritious in any way.
But all I can do right now is breathe. And wait. And be as strong as I can be for my husband, who is the strongest man in the world.
self care?
The past few months have been a whirlwind. Of what, I’m not sure. But it feels like every day the minutes slip away and I’m constantly fighting to be more efficient, to use time wisely, to check all the boxes of ‘things to do’ … and yet, I still manage to feel constantly behind.
A few weeks ago on my Instagram feed (the MS one ~ ilooknormal) I posted about self care. That I hadn’t meant for 2018 to be shaped by it, but somehow, that’s what has happened. For a few weeks I’ve been going to the chiropractor three times a week. It is actually crazy how much that changes your life. And for two months I’ve also been hoofing it to yoga multiple times a week. Plus riding the bike. Plus switching to a Keto diet (um, yeah, I’m not super good at it, but it definitely has its benefits).
Let’s rewind here a minute.
I am not working. So it makes it easier for me to prioritize yoga and chiropractic care and sleep and cooking every day , etc., etc., etc. But after all these weeks of ‘taking care of myself’ I feel a little lost. I mean, I know that the things I am doing are good things. My body does feel better. But, if I had a job, or any other obligation whatsoever, how could I possibly fit all this stuff in?
Sometimes I wonder if it’s the fatigue. If ‘normal’ people just have more hours in the day because their bodies require less sleep. Or, even if they do require as much sleep as I do, they just skip it and manage to be okay. That is not the case for me. Two nights ago I slept for about six and half or seven hours and spent the following day feeling like I was going to die. Eight hours isn’t negotiable for me. It is a requirement. Nine is better. Otherwise all the carefully placed cards in this little house of mine crumble to the ground in an instant.
So.
How do I prioritize this ‘self care’ (most of which is physical) and ALSO manage not to lose my mind?
This is an interesting conundrum.
For the first time in more than a decade, I went to a therapist. This was prompted by my neurologist who pondered during my last appointment if the troubles I was facing in my MS journey were not, as it happened, brought on physically but rather, mentally.
That’s a cold bucket of water to the head if there ever was one. I’d been so focused on the physical side of my disease that I’d completely forgotten that the insidious monster doesn’t discriminate when it comes to triggers. And how (this I asked out loud) could the issue be mental when I’d left my job (y’know, the one with all the stress and anxiety and b.s.) nearly fifteen months earlier?
Mmmmmm.
So, self care is about a little bit more than a chiropractor and yoga and a Keto diet.
To me, right now, it’s about finding an anchor. And figuring out the direction of the wind. I feel physically better since I’ve been doing all of ‘the stuff’ but I also feel adrift and confused and lost. I’m not sure what I’m doing and at 38, retirement doesn’t feel right. So how can I leverage all this stuff and do something I love?
Yeah, I haven’t figured that out yet.
I love writing, but I never seem to find the time. I love cooking, but at the end of the day (when most of the cooking is done in our house) all I want to do is curl up on the couch and be quiet and still. I love traveling and restaurants and using my brain. But what with all the hot yoga and bike riding and chiro appointments I am too tired to even contemplate doing anything else. And if I went back to work full time, I’d give up everything that I have found to help control the disease. So, that’s a little like my own private Sophie’s Choice.
Anyway. My goal is to get back to this blog more regularly. Like Stephen King wrote in his amazing book “On Writing,” you really need to do it every day. Keep the muscles fresh. Keep honing the skill. Maybe, while I’m doing all this, something will clarify and I’ll find my way. Until then, I’m on my self care journey & I’m hoping that it keeps getting the job done.
energy
I was inspired recently to revisit a book I began reading a few years ago and never finished. I bought it because Gwyneth Paltrow wrote the forward (and I love Gwyneth Paltrow) and the book was supposedly about weight loss. Something I was struggling with at the time.
It isn’t about weight loss at all. I mean, it is. But it isn’t. And I will confess that I never finished it. But the ideas within it I carry with me every day. Because the book is about … um, enlightenment. Sort of. I’m struggling to properly articulate what Dr. Sadeghi writes about. Because it all sounds cheesy. And yet, to me, the book is so far from actually being cheesy I really don’t want to do it a disservice. So I’ll use Dr. Sadeghi’s words — the book is about self love.
When I began my job a month ago, my District Sales Coordinator handed me (and everyone on our team) a book called “The Energy Bus.” I happen to love books like that, so I was looking forward to cracking it open. But before I had a chance, she and I talked about it. And I heard myself talking about Dr. Sadeghi’s principles with such conviction I knew I had to go back and finish “Within.” (**As I read both books, I am in awe of how similar many of their ideas are — just presented in slightly different ways and in different contexts. It makes me smile.)
I don’t know that I have always tried to evolve as I’ve grown but I think, looking back, it happened without my conscious awareness of it. John (the hubs) always teases me that early every year I go through my “Self Help” phase. I find a book and read it cover to cover in a matter of days and then try to apply principles and new practices to my (and John’s!) life. I find comfort in it. Trying to be more aware, trying to be better. Trying to understand life & myself more. I loved so many ideas in Dr. Sadeghi’s book (y’know, the part I read). He talks about self love, yes, but he also talks about energy and the power of our mind & heart.
When you have an incurable disease like mine (or maybe any struggle, really) there’s a different perspective about health. Or, to be more precise, wellness. And more and more, I read articles about the power of positivity in the workplace, in life, in healing. Its pretty profound. And I can say from personal experience that where my mind is at very much affects my physical wellness. My first neurologist handed me information on four different drug therapies when I received my MS diagnosis. He told me to read about each one, and come back and tell him which medicine I wanted to take. He said he didn’t like picking medicines for MS patients because he believed that if I believed in the medicine there was a greater chance of it being successful. In retrospect, that was exceptionally powerful and has (clearly) stayed with me. And the medicine I picked did work. It just had rough side effects. The therapy I am on now my current neurologist prescribed to me three times before I went in and had my first infusion. And I only went in after sitting in an office with him for hours debating the pros and cons, discussing the potential health risks. I left believing it was the best option for me and would work. And it has.
I guess what I’m getting at, in a very fractured manner, is that I have deep faith and belief in the power of our thoughts. Being positive and optimistic are part of the battle. Every day. I can physically feel the difference when I am down or feeling discouraged. I can feel it if someone near me is full of angry, negative emotions. We are all energy. And our energy feeds off other’s energy. Everything is interrelated. Its profound to me, and mind-blowing, and gives me infinite faith in life. It helps me in my journey every day. To make better, smarter choices. To eat better food. To take care of my body. To focus my mind on constructive, positive, enriching and nurturing things.
starting again
When I left my job last January, I didn’t really have any idea what I was going to do. I was quite certain that I would spend February sleeping & watching junk TV (mission accomplished) but after that … it was sort of nebulous.
Last year was a good year. I found myself again, I worked through some things. I decided I wasn’t actually that bad of a person. I’d just maybe spent too much time in toxic situations surrounded by toxic people. (Let’s take a time out for a minute — I don’t think I really understood what a toxic person was until I understood myself, so that’s kinda the catch with toxic people. They come in all shapes and sizes and their toxicity is different depending on who they are interacting with … so it can get complicated.) But the thing is folks — anyone who makes you feel bad, who makes you doubt yourself, who is constantly stating the negative… probably toxic.
Also, being around people whose values, morals, ideas of life matched mine in a lot of ways — much healthier than being told all the time that I was doing it all wrong.
I think I’ve distracted myself with this train of thought. So I’m going to diverge for a minute. Just because my values and morals are different from yours doesn’t make mine right and yours wrong. It doesn’t even classify them. It’s just that I see life one way, and you see it another. And both those ways could be awesome. They could be fulfilling and exciting and full of adventure and learning and fun. It’s just that I prefer to do things my way, and you prefer to do them your way. If either of us start pointing fingers and belittling the other — that’s when it gets bad. I don’t necessarily agree with a lot of things. But it isn’t my place to tell you that YOU can’t do them. And in turn, you shouldn’t criticize my life because I make different choices. I’m not trying to solve the worlds problems right now. But I think this past year has given me a lot of perspective that I had lost.
Right, so my point of this post.
Next week I start a new job. It’s a scary job and it is completely outside my comfort zone. It isn’t like anything I’ve ever done in my entire life. I am terrified. But I am also hoping that this new step allows me to have purpose, earn an income and do something to help other people. Sitting at home for a year really helps you figure out your drive (or lack thereof). It tells you what you need to feel happy and fulfilled. And I’m hoping that going back to work and being part of society again is something I am able to handle without sacrificing everything I’ve worked so hard on this past year.
and now, we are here
This month has been a little crazy for me. Sooooo many MS appointments, needles in my arms, big magnets, life-saving drugs, etc etc.
Today, Facebook reminded me that a year ago, I left my old employer. It blew my mind that it has both been a year, and been.a.year! So much has changed.
To be fair, I probably should have left a lot earlier than I did. I don’t think I had any concept of how wildly unhappy I was until several months of decompression had occurred. Suddenly I wasn’t angry any more, I wasn’t constantly stressed out about things I couldn’t control and I began to see my life a little more clearly.
Multiple sclerosis is pretty serious. I mean, it is but it also isn’t. I think I’m just used to it by now. It’s just how my waking hours are shaped every day. I learn, I make adjustments, i forge on. I don’t think I spent nearly enough time thinking about that and how my life had changed with my diagnosis until I wasn’t working any more. I mean, my job controlled my whole life. It was always priority number one.
And let’s be honest. For years, it was a one in a million job. I had lucked out. But then, suddenly, it wasn’t anymore. And I had to call it. I don’t regret that.
I know this post is a little bit of a ramble through my mind, but everyone’s journey is different. Just like everyone’s MS is different. We all get up in the morning and do our best … and sometimes that’s enough and sometimes it isn’t. When I lie down to sleep every night (well, y’know, most nights when the fatigue hasn’t totally clobbered me) I do an inventory of the day. Did I drink enough water? Did I eat well? Did I exercise? Did the chores get done, the laundry folded, the groceries bought and put away? Did the damn floor get cleaned?!? (It is the bane of my existence). Did I moisturize, brush my teeth (this one is a little hard for me to forget, I’m manic about brushing my teeth!) did I take care of all my MS stuff …. I mean, the list doesn’t end. I’ve usually fallen asleep before I get through it.
MS makes you think about other things as well, when you’re ready to think about them. It makes you think about how you spend your time, how you spend your money, what you prioritize, who your real friends are. It helps you to shape your life in a better way — both mentally and physically. Possibly emotionally as well, but I’m not sure I’ve gotten there.
There are a million ways to live a life. When I left Z, I worried that I’d made the worst decision. That I would look back and regret it. I justified. I got angry. I twisted everything up and over-examined it. But you know what really healed all the pain that it had caused me?
Time.
Time away. Time pursuing other dreams. Time that rolled on and moved away. And suddenly, all the angst, all the introspection, all the heartache and self-doubt and stress and anxiety that those seven years had caused me feels very far away. And I feel free.
only numbers
I turned 38 earlier this month.
I’m pretty sure that every member of my family ‘teased’ me about my obsession with numbers at one point or another (this year, and every year …. this month and every month). But I think I see life like a big, gridded calendar and knowing where everyone lies helps to quiet the never ceasing chaos of my brain.
Here’s the thing. I’m okay with being 38. I’m actually better than okay with being 38. It fits me. I fit into the grid nicely on December 12 and currently, at the age of 38. I’ve enjoyed my 30s. I don’t look my age (thank you Rodan + Fields and not having children) but even if I did, I think I’d be okay at 38. Every moment in life is a learning moment, something that helps you (hopefully!) become better, more thoughtful, more well-rounded. Something that helps you appreciate where you are at this very moment.
Today, my mother turns 70. I’m fairly certain she wouldn’t love me saying that. Most people don’t (although I routinely say people’s ages as I know them and their relationship to my own age — even if it’s in days, minutes, hours or years).
My mother is the best that seventy combined years has to offer. She is thoughtful, kind, intelligent, funny, insightful, open, understanding, opinionated, strong … she has a distinct voice not only in my world, but in THE world. She is measured in her responses, but that doesn’t prevent her from being cutting when she deems it appropriate (or necessary). She believes in things and stands by them. She soldiers on through the most unfair, the toughest of odds and she does it with a smile. Her eyes still sparkle, she still gets dressed up, she still has the delight of a child when something new, or unexpected surprises her.
She looked at me across the dinner table last night, and gazed down at her son, my little brother, seated at the end of the table, and I could see the love and pride in her eyes. She did an exceptional job raising us — she was the most lovely, most creative, most perfect mother a child could ask for. She treated us like people (she always said it was because she was not meant to be a mother, but I think it’s because she absolutely was meant to be a mother — our mother). She taught us, and took us on adventures, and made everything seem interesting and fun. She encouraged learning, and welcomed us onto her bed at night to read stories (during which she did all the voices). She made huge sacrifices we didn’t understand and she never burdened us with in order to give us the life we had as children.
As adults she has listened, supported us, allowed us to stretch our wings and both fall and fly. She has embraced our chosen partners (even dusting off her French to speak to David’s lady in her native tongue).
She is — quite simply — exquisite.
And despite my bizarre obsession with numbers, that’s all they really are. Just numbers. They don’t define an age, a person. They merely track time.
Anyway, today and every day I love my mummy. My mama bear. At every age. At any age.
D5 Creation